Evidence map›Paper›PMID 41488462›Full record

ArticleFrontiers in cardiovascular medicine2025

Establishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age.

Manuela A Oestereicher, Christopher S Ward, Elida Schneltzer, Susan Marschall, Helmut Fuchs, Valerie Gailus-Durner, Ghina Bou About, Mohammed Selloum, Hamid Meziane, Michelle Stewart and 20 more

Erratum issuedAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. EchoVisuALL: From Echocardiography to Gene Discovery.bioRxiv : the preprint server for biology · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Manuela A Oestereicher *Institute of Experimental Genetics and German Mouse Clinic, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Christopher S Ward *Université de Strasbourg, CNRS, INSERM, Institute de la Clinique de la Souris, PHENOMIN, ILLKIRCH, France.
Elida SchneltzerInstitute of Experimental Genetics and German Mouse Clinic, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Susan MarschallInstitute of Experimental Genetics and German Mouse Clinic, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Helmut FuchsInstitute of Experimental Genetics and German Mouse Clinic, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Valerie Gailus-DurnerInstitute of Experimental Genetics and German Mouse Clinic, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Ghina Bou AboutThe Mary Lyon Centre and MRC Harwell, Harwell Campus, Oxfordshire, United Kingdom.
Mohammed SelloumThe Mary Lyon Centre and MRC Harwell, Harwell Campus, Oxfordshire, United Kingdom.
Hamid MezianeThe Mary Lyon Centre and MRC Harwell, Harwell Campus, Oxfordshire, United Kingdom.
Michelle StewartEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
Lydia TeboulEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
Clare NorrisEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
Dale PimmEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
Marina KanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.
Federico López GómezDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.
Robert WilsonDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.
Mayra MonroyDepartment of Integrative Physiology, Baylor College of Medicine, Houston, TX, United States.
Sheraz PashaDepartment of Integrative Physiology, Baylor College of Medicine, Houston, TX, United States.
Eva ZabrodskaAdvanced Technology Cores, Baylor College of Medicine, Houston, TX, United States.
Jan ProchazkaAdvanced Technology Cores, Baylor College of Medicine, Houston, TX, United States.
David Pajuelo RegueraAdvanced Technology Cores, Baylor College of Medicine, Houston, TX, United States.
Zuzana NichtovaAdvanced Technology Cores, Baylor College of Medicine, Houston, TX, United States.
Yann HeraultThe Mary Lyon Centre and MRC Harwell, Harwell Campus, Oxfordshire, United Kingdom.
Sara WellsEuropean Molecular Biology Laboratory-European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
Helen ParkinsonDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.
Jason D HeaneyCzech Centre for Phenogenomics, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Radislav SedlacekAdvanced Technology Cores, Baylor College of Medicine, Houston, TX, United States.
Xiang GaoSKL of Pharmaceutical Biotechnology and Model Animal Research Center, Collaborative Innovation Center for Genetics and Development, Nanjing Biomedical Research Institute, Nanjing University, Nanjing, China.
Martin Hrabe de AngelisInstitute of Experimental Genetics and German Mouse Clinic, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Nadine SpielmannInstitute of Experimental Genetics and German Mouse Clinic, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.

Funding

The Jackson Laboratory Knockout Mouse Production and Phenotyping Project (JAX KOMP2)UM1OD023222 · OD · JACKSON LABORATORY · PI ROBERT E BRAUN, Stephen A Murray · 2016 to 2026
$47.2M
KOMP2-Phase3 Production and Phenotyping by the DTCC Consortium TCP Transfer to UC DavisUM1OD023221 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KC KENT LLOYD · 2016 to 2026
$45.7M
Mouse Phenotyping Informatics Infrastructure - MP12UM1HG006370 · NHGRI · EUROPEAN MOLECULAR BIOLOGY LABORATORY · PI Pilar Cacheiro Martinez, Helen Elizabeth Parkinson · 2016 to 2026
$20.4M
KOMP Phase II Mouse Production and CryopreservationU42OD011175 · OD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LLOYD, KC KENT · 2012 to 2015
$18.9M
KOMP Phase II Mouse PhenotypingU54HG006364 · NHGRI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LLOYD, KC KENT · 2011 to 2015
$16.3M
NHGRI NIH HHS U54 HG006364NHGRI NIH HHS UM1 HG006370NIH HHS U42 OD011175NIH HHS UM1 OD023221NIH HHS UM1 OD023222
6 · The paper itself

Abstract

Introduction: Mouse models play a critical role in cardiology research, offering valuable insights into the molecular mechanisms, genetics, and potential treatments for cardiovascular diseases. However, the ability to transfer findings in mice between studies is limited by the absence of standardized protocols and valid reference values for the assessment of normal cardiac function in mice. This study aims to establish comprehensive transthoracic echocardiography (TTE) reference ranges for mice, particularly focusing on C57BL/6N wild-type controls. Methods: The study, which includes data from over 15,000 mice through the International Mouse Phenotyping Consortium (IMPC), highlights how variables such as sex, age, body weight, and anesthesia impact TTE parameters. Results: The findings showed that anesthesia is the primary predictor of variability in cardiac function. Isoflurane- and tribromoethanol-anesthetized mice presented with modified cardiac function compared with conscious mice. In addition, we observed minimal sex differences in cardiac morphology and function, except for small variations influenced by anesthesia. The effects of aging on cardiac function were modest, characterized by a decrease in heart rate and subtle changes in ventricular dimensions without evidence of pathological remodeling, possibly attributable to disease-free cardiovascular aging. Discussion: Validation of the reference ranges across multiple mouse strains showed that these values provide a reliable baseline for experiments involving cardiac function in mice. The data underscore the importance of using anesthesia-specific reference values when interpreting TTE results, ensuring robust comparisons in genetic and pharmacological studies. These reference ranges serve as quality assurance tools for future cardiac studies in mice, offering insights into typical TTE parameter values, supporting the detection of experimental perturbations, and contributing to more effective translation of findings from mice to humans.

Indexed as

anesthesia effects on cardiac functionC57BL/6N mouse modelcardiovascular phenotypingmouse cardiac reference rangestransthoracic echocardiography (TTE)

Identifiers

PMID41488462
PMCPMC12757355

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.